Optimizing and understanding semantic feature analysis treatment for aphasia: A randomized controlled comparative-effectiveness trial
Optimizing and understanding semantic feature analysis treatment for aphasia: A randomized controlled comparative-effectiveness trial
批准号:
10688141
负责人:
Michael Walsh Dickey
金额:
$46.01万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-01 至 2024-08-31
关键词:
AddressAffectAftercareAlzheimer&aposs DiseaseAmericanAphasiaAreaBehavioralBilateralBrainBrain imagingBrain regionCategoriesClinicalCognitiveCommunicationCommunication impairmentDataEquationEquilibriumFunctional Magnetic Resonance ImagingFundingGenerationsGrowthHomologous GeneHourImpairmentLanguageLanguage TestsLeftLesionMaintenanceMalignant NeoplasmsMeasuresMethodsModelingNamesNeurocognitiveOutcomeParticipantPatientsPerformancePersonsProcessPsycholinguisticsRandomizedReportingResolutionResponse GeneralizationRestRetrievalSemanticsSiteSpeechStandardizationSystemTest ResultTestingTimeTrainingVariantVisualWord Processingclinically relevantcomparative effectiveness studycomparative effectiveness trialefficacious treatmentfollow-uphealth related quality of lifeimprovedimproved outcomelanguage processinglexicallexical retrievalneural correlateneuromechanismnovelphonologypost interventionpredicting responserecruitremediationresponsesample fixationsecondary outcomesemantic processingsuccesstreatment responsetreatment trialvisual tracking
中文摘要
点击翻译按钮获取中文摘要
英文摘要
This randomized comparative effectiveness trial examines whether active manipulation of a key component
of semantic feature analysis (SFA) treatment for word-finding difficulty in aphasia improves outcomes. The key
component in question is the number of semantic features that persons with aphasia are asked to generate on
each treatment trial. Study participants (n=40) will be recruited and randomized to receive either a many-
features version of SFA or a few-features version. In the many-features condition, participants will be asked to
generate 11 semantic features for each word practiced. Participants assigned to the few-features condition will
be asked to generate 5 features for each word practiced. The total treatment time will be equated in the two
conditions. Because each trial will take less time in the few-features condition, participants in this group will
cycle through the lists of treated items more often, providing them with more opportunities to practice the
phonological form of the targets, at the expense of more elaborated feature generation practice.
Correspondingly, the many-features group will receive more practice generating semantic features, at the
expense of few opportunities to practice the target word forms.
Study participants will be housed locally at the Pittsburgh site for five weeks during which they will receive
60 hours of SFA treatment with pre- and post-treatment assessment of their ability to name pictures of treated
and untreated, semantically related nouns. Other secondary outcomes, including measures of connected
speech and patient-reported communication ability will also be collected. In order to address unresolved
questions about the underlying cognitive and neural mechanisms of SFA, participants will also receive
concurrent pre- and post-treatment assessment of automatic word processing ability using eye-tracking
methods and functional magnetic resonance imaging (fMRI). Participants will also be asked to return to
Pittsburgh for one-month follow-up language, eye-tracking, and fMRI testing.
The language testing results will be used to determine the appropriate balance of feature generation
practice vs. word form practice to optimize SFA outcomes. The eye-tracking results will be used to infer
whether SFA’s positive effects can be attributed to improved activation of lexical-semantic representations,
improved ability to inhibit competing representations, or both. The fMRI results will be used to identify the
brain networks and activation changes associated with changes in naming ability resulting from SFA. This
study will provide theoretically and clinically relevant information about how aphasia treatment should be
delivered and the neurocognitive mechanisms underlying its effects.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Optimizing and understanding semantic feature analysis treatment for aphasia: A randomized controlled comparative-effectiveness trial
-
批准号:10000877
-
项目类别:
-
资助金额:$55.27万
-
财政年份:2019
-
负责人:Michael Walsh Dickey
-
依托单位:
Optimizing and understanding semantic feature analysis treatment for aphasia: A randomized controlled comparative-effectiveness trial
-
批准号:10244949
-
项目类别:
-
资助金额:$55.27万
-
财政年份:2019
-
负责人:Michael Walsh Dickey
-
依托单位:
Optimizing and understanding semantic feature analysis treatment for aphasia: A randomized controlled comparative-effectiveness trial
-
批准号:10610579
-
项目类别:
-
资助金额:$1.02万
-
财政年份:2019
-
负责人:Michael Walsh Dickey
-
依托单位:
Optimizing and understanding semantic feature analysis treatment for aphasia: A randomized controlled comparative-effectiveness trial
-
批准号:10466962
-
项目类别:
-
资助金额:$48.14万
-
财政年份:2019
-
负责人:Michael Walsh Dickey
-
依托单位:
Dosage and predictors of naming treatment response in aphasia
-
批准号:9136710
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2013
-
负责人:Michael Walsh Dickey
-
依托单位:
Dosage and predictors of naming treatment response in aphasia
-
批准号:8984834
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2013
-
负责人:Michael Walsh Dickey
-
依托单位:
Neural Bases of Verb-Argument Processing
-
批准号:8451368
-
项目类别:
-
资助金额:$30.63万
-
财政年份:2012
-
负责人:Michael Walsh Dickey
-
依托单位:
Neural Bases of Verb-Argument Processing
-
批准号:8297054
-
项目类别:
-
资助金额:$32.85万
-
财政年份:2012
-
负责人:Michael Walsh Dickey
-
依托单位:
Neural Bases of Verb-Argument Processing
-
批准号:8642637
-
项目类别:
-
资助金额:$32.21万
-
财政年份:2012
-
负责人:Michael Walsh Dickey
-
依托单位:
Research Symposium in Clinical Aphasiology
-
批准号:9944481
-
项目类别:
-
资助金额:$3.33万
-
财政年份:2003
-
负责人:Michael Walsh Dickey
-
依托单位:
Research Symposium in Clinical Aphasiology
-
批准号:9199223
-
项目类别:
-
资助金额:$3.33万
-
财政年份:2003
-
负责人:Michael Walsh Dickey
-
依托单位:
海外基金